BEUDAMED
    11 results · 46ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Status: Malfunction ×

    APEX KNEE SYSTEM

    FDA Adverse Event
    Malfunction ·OMNI LIFE SCIECE, INC.·Product code JWH·December 22, 2021

    SHELL INSERTER W/O ROTATION CONTROL

    FDA Adverse Event
    Malfunction ·OMNI LIFE SCIENCE, INC.·Product code LXH·June 16, 2010

    APEX MODULAR HIP SYSTEM

    FDA Adverse Event
    Malfunction ·OMNI LIFE SCIENCE, INC.·Product code LPH·December 23, 2009

    APEX K1 HIP STEM

    FDA Adverse Event
    Malfunction ·OMNI LIFE SCIENCE, INC.·Product code LPH·January 20, 2011

    APEX HIP SYSTEM BIPOLAR HEAD

    FDA Adverse Event
    Malfunction ·OMNI LIFE SCIENCE INC.·Product code KWY·July 15, 2009

    APEX MODULAR HIP STEM

    FDA Adverse Event
    Malfunction ·OMNI LIFE SCIENCE INC.·Product code KWY·May 22, 2008

    APEX DOVETAIL TIBIAL TRAY

    FDA Adverse Event
    Malfunction ·OMNI LIFE SCIENCE INC·Product code HSH·September 18, 2008

    OMNI TRAY TRIAL HANDLE

    FDA Adverse Event
    Malfunction ·OMNI LIFE SCIENCE, INC.·Product code LXH·September 9, 2008

    APEX K2 BROACH

    FDA Adverse Event
    Malfunction ·OMNI LIFE SCIENCE, INC.·Product code HTQ·August 7, 2006

    ALL POLY PATELLA

    FDA Adverse Event
    Malfunction ·OMNI LIFE SCIENCE, INC.·Product code JWH·April 27, 2015

    CUSA EXCEL 23KHZ CEM NOSECONE

    FDA Adverse Event
    Malfunction ·INTEGRA NEUROSCIENCES PR·Product code LFL·June 26, 2015